Therapeutic Stockings to Prevent Foot Ulcers
Primary Purpose
Diabetes
Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Standard therapy
PFC Stockings
Sponsored by
About this trial
This is an interventional prevention trial for Diabetes focused on measuring diabetes, foot ulcer prevention, therapeutic stockings
Eligibility Criteria
Inclusion Criteria:
- Men or women 18 years old or older
- Diagnosis of Diabetes Mellitus*
- History of diabetes related foot ulceration
Spanish-speaking subjects will be eligible to participate.
Exclusion Criteria:
- Active Charcot Arthropathy
- Gangrene, active infection
- Midfoot or higher level amputation
- Alcohol or substance abuse within 6 months
- Unreliable, unwilling or unable to comprehend informed consent
Sites / Locations
- Parkland Health & Hospital Systems
- UT Southwestern Medical Center at Dallas
- Scott & White
- University of Manchester
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Standard therapy
PFC Stockings
Arm Description
Standard therapy consisting of education, regular foot care and protective shoes and insoles. The standard therapy group will use the stockings they normally wear.
The stocking therapy group will be given PFC shear reducing stockings to wear.
Outcomes
Primary Outcome Measures
Number of Participants Who Developed Foot Ulcer During Study Time Frame
An ulceration will be defined as full thickness loss of epidermis and dermis or involvement of deeper structures.
Secondary Outcome Measures
Full Information
NCT ID
NCT01221194
First Posted
October 13, 2010
Last Updated
August 12, 2020
Sponsor
University of Texas Southwestern Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
1. Study Identification
Unique Protocol Identification Number
NCT01221194
Brief Title
Therapeutic Stockings to Prevent Foot Ulcers
Official Title
Therapeutic Stockings to Prevent Foot Ulcers
Study Type
Interventional
2. Study Status
Record Verification Date
August 2020
Overall Recruitment Status
Completed
Study Start Date
October 2010 (undefined)
Primary Completion Date
February 2016 (Actual)
Study Completion Date
March 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center
Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No
5. Study Description
Brief Summary
To evaluate the efficacy of a therapeutic stockings (Protective Foot Care stockings, PFC) in reducing the incidence of diabetic foot pathology among high-risk patients.
To evaluate perceived health-related quality of life as compared to guideline directed usual care in patients who use the PFC stockings.
Detailed Description
We will identify a cohort of high-risk diabetic patients and assign them to two treatment groups. We plan to enroll patients from three sites: Scott and White Hospital in Temple Texas, Manchester Royal Infirmary, UK , and Trinity College Dublin at St James Hospital.. The two treatment arms will involve a Standard Therapy Group, and a Stocking Therapy Group. The Stocking Therapy group will use the special padded and friction reducing stockings in their standard shoes during the course of the study. Patient enrollment will occur over a one-year period. All patients will be followed for 30 months. The Standard Therapy Group will receive therapeutic shoes, standard insoles, patient education and regular foot evaluations by a physician every 10-12 weeks. The Stocking Therapy Group will receive standard therapy as described above but use the special stockings instead of their usual hose. The investigator at each site will be blinded regarding the treatment.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetes
Keywords
diabetes, foot ulcer prevention, therapeutic stockings
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
381 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Standard therapy
Arm Type
Active Comparator
Arm Description
Standard therapy consisting of education, regular foot care and protective shoes and insoles. The standard therapy group will use the stockings they normally wear.
Arm Title
PFC Stockings
Arm Type
Active Comparator
Arm Description
The stocking therapy group will be given PFC shear reducing stockings to wear.
Intervention Type
Behavioral
Intervention Name(s)
Standard therapy
Intervention Description
Standard therapy consisting of education, regular foot care and protective shoes and insoles. The standard therapy group will use the stockings they normally wear.
Intervention Type
Device
Intervention Name(s)
PFC Stockings
Intervention Description
A pressure and friction reducing stocking. The novelty of the PFC Sock stems from its innovative double layer structure and technological fibre composition. These simultaneously and significantly reduce both pressure and friction in a format that is practical for everyday wear with therapeutic shoes in high-risk cases.
Primary Outcome Measure Information:
Title
Number of Participants Who Developed Foot Ulcer During Study Time Frame
Description
An ulceration will be defined as full thickness loss of epidermis and dermis or involvement of deeper structures.
Time Frame
30 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Men or women 18 years old or older
Diagnosis of Diabetes Mellitus*
History of diabetes related foot ulceration
Spanish-speaking subjects will be eligible to participate.
Exclusion Criteria:
Active Charcot Arthropathy
Gangrene, active infection
Midfoot or higher level amputation
Alcohol or substance abuse within 6 months
Unreliable, unwilling or unable to comprehend informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lawrence Lavery, DPM
Organizational Affiliation
UT Southwestern Medical Center at Dallas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parkland Health & Hospital Systems
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
Facility Name
UT Southwestern Medical Center at Dallas
City
Dallas
State/Province
Texas
ZIP/Postal Code
75390
Country
United States
Facility Name
Scott & White
City
Temple
State/Province
Texas
ZIP/Postal Code
76502
Country
United States
Facility Name
University of Manchester
City
Manchester
Country
United Kingdom
12. IPD Sharing Statement
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Therapeutic Stockings to Prevent Foot Ulcers
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